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D H Geschwind

Showing results (21-30 of 70) with videos related to

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 1, 1995
TOAD-64, a gene expressed early in neuronal differentiation in the rat, is related to unc-33, a C. elegans gene involved in axon outgrowthJ E Minturn, H J Fryer, D H Geschwind, et al.
Neurology|March 1, 1995
Sneddon's syndrome is a thrombotic vasculopathy: neuropathologic and neuroradiologic evidenceD H Geschwind, M FitzPatrick, P S Mischel, et al.
Molecular Psychiatry|November 23, 2011
QTL replication and targeted association highlight the nerve growth factor gene for nonverbal communication deficits in autism spectrum disordersA T-H Lu, J Yoon, D H Geschwind, et al.
Mental Retardation and Developmental Disabilities Research Reviews|July 19, 2000
Neurobehavioral phenotype of Klinefelter syndromeD H Geschwind, K B Boone, B L Miller, et al.
Archives of Neurology|July 15, 1999
Inheritance of frontotemporal dementiaT W Chow, B L Miller, V N Hayashi, et al.
Dementia and Geriatric Cognitive Disorders|August 7, 1999
Tau mutations in frontotemporal dementiaK C Wilhelmsen, L N Clark, B L Miller, et al.
Molecular Psychiatry|March 20, 2013
Genes for endosomal NHE6 and NHE9 are misregulated in autism brainsM Schwede, K Garbett, K Mirnics, et al.
Brain Research. Developmental Brain Research|November 22, 1996
Identification and characterization of novel developmentally regulated proteins in rat spinal cordD H Geschwind, G M Kelly, H Fryer, et al.
Archives of Neurology|November 16, 2001
The SCA12 mutation as a rare cause of spinocerebellar ataxiaJ A Cholfin, M J Sobrido, S Perlman, et al.
American Journal of Human Genetics|April 1, 1997
The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxiaD H Geschwind, S Perlman, C P Figueroa, et al.
Pageof 7

Showing results (21-30 of 70) with videos related to

Sort By:
Pageof 7
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 1, 1995
TOAD-64, a gene expressed early in neuronal differentiation in the rat, is related to unc-33, a C. elegans gene involved in axon outgrowthJ E Minturn, H J Fryer, D H Geschwind, et al.
Neurology|March 1, 1995
Sneddon's syndrome is a thrombotic vasculopathy: neuropathologic and neuroradiologic evidenceD H Geschwind, M FitzPatrick, P S Mischel, et al.
Molecular Psychiatry|November 23, 2011
QTL replication and targeted association highlight the nerve growth factor gene for nonverbal communication deficits in autism spectrum disordersA T-H Lu, J Yoon, D H Geschwind, et al.
Mental Retardation and Developmental Disabilities Research Reviews|July 19, 2000
Neurobehavioral phenotype of Klinefelter syndromeD H Geschwind, K B Boone, B L Miller, et al.
Archives of Neurology|July 15, 1999
Inheritance of frontotemporal dementiaT W Chow, B L Miller, V N Hayashi, et al.
Dementia and Geriatric Cognitive Disorders|August 7, 1999
Tau mutations in frontotemporal dementiaK C Wilhelmsen, L N Clark, B L Miller, et al.
Molecular Psychiatry|March 20, 2013
Genes for endosomal NHE6 and NHE9 are misregulated in autism brainsM Schwede, K Garbett, K Mirnics, et al.
Brain Research. Developmental Brain Research|November 22, 1996
Identification and characterization of novel developmentally regulated proteins in rat spinal cordD H Geschwind, G M Kelly, H Fryer, et al.
Archives of Neurology|November 16, 2001
The SCA12 mutation as a rare cause of spinocerebellar ataxiaJ A Cholfin, M J Sobrido, S Perlman, et al.
American Journal of Human Genetics|April 1, 1997
The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxiaD H Geschwind, S Perlman, C P Figueroa, et al.
Pageof 7